Our company’s knowledge and experience for what concerns inhalers assembly is unrivaled. We offer a highly versatile inhaler assembly line, with a flexible dedicated platform and the possibility to choose between Automatic or Semi-Automatic running mode.
100% weigh check, plus all of our platforms are easy to clean and made according to the highest standards for reduced footprints, allowing Inhalers to be manufactured efficiently, reliably and cost-effectively.
IMA Automation is deeply experienced in the assembly of pens and auto-injectors: from automatic denesting systems for pre-filled syringes to dosing mechanism, other than p\ower-pack assembly and final product assembly including drug manipulation. Turnkey solutions are also offered, together with packaging equipment, if required.
IMA Automation is deeply experienced in the assembly of pens and auto-injectors: from automatic denesting systems for pre-filled syringes to dosing mechanism, other than power-pack assembly and final product assembly including drug manipulation. Turnkey solutions are also offered, together with packaging equipment, if required.
Thanks to the study and optimization of existing platforms, IMA Automation has developed fully customized process lines for the handling of contact and blister packaging.
Lines are designed to implement robotizing, filling, laser and inspection systems, in order to duly execute lens releasing, washing and packaging operations. This also ensures high versatility in the handling of different sizes of lenses, thanks to quick mechanical & control changeovers.
We supports solutions for each step of your device development from process understanding to operation. Our goal is to develop with our customer a comprehensive manufacturing science of the medical device by following principles of Quality-by-Design (QbD).
Together we understand process variability impacting your device and put in process controls in place to meet your expected device quality.
Validation is a must-do and being aware of the demanding requirements of the medical industry ensures the safety, purity and
effectiveness of your medical device and enables you to complete all the necessary documentation requirements.
Our flexible modular approach, fully compatible with the GAMP 5 methodology, is carefully designed to fit each customer validation strategy and specific needs, minimizing time while effi ciently placing “your device to market”.